Allele Registry

Canonical Allele Identifier: PA2827781762

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000443388

ClinVar Variation:

393038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Asn357Tyr	CA16603944 NM_001353957.2:c.1069A>T